# K041243: Dover Red Rubber Robinson Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Tyco Healthcare
- Decided: Jul 7, 2004 after 57 days
- Product code: KOD (Catheter, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Tyco Healthcare/Kendall DOVER RED RUBBER ROBINSON Catheter: named in the summary without a submission number

## Most influential descendants
- K251864: Rubber Utility Catheter (2026), 0 descendants of its own

## Indications for use
The proposed device is intended for use in the drainage of urine from the urinary bladder. The product is intended for intermittent catheterization on patients who are not capable of voluntary urination. This product is not designed for use as an indwelling catheter.

Source page: https://510kreport.com/device/K041243
Methodology: https://510kreport.com/methodology